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Hospital & Community Psychiatry|July 1, 1991
Men's changing social roles in the 1990s: emerging issues in the psychiatric treatment of menL J Dickstein, T S Stein, J H Pleck, et al.Human Genetics|November 3, 1998
A novel locus for Leber congenital amaurosis on chromosome 14q24D W Stockton, R A Lewis, E B Abboud, et al.Brain : a Journal of Neurology|June 27, 2000
Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1AK M Krajewski, R A Lewis, D R Fuerst, et al.Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|July 13, 2004
Self-assembled uniaxial and biaxial multilayer structures in chiral smectic liquid crystals frustrated between ferro- and antiferroelectricityV P Panov, N M Shtykov, A Fukuda, et al.American Heart Journal|July 1, 1983
Ethmozine suppression of single and repetitive ventricular premature depolarizations during therapy: documentation of efficacy and long-term safetyC M Pratt, S C Yepsen, A A Taylor, et al.American Journal of Human Genetics|February 11, 1999
Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt diseaseR A Lewis, N F Shroyer, N Singh, et al.Journal of Immunology (Baltimore, Md. : 1950)|May 15, 1986
Enhancement by monokines of leukotriene generation by human eosinophils and neutrophils stimulated with calcium ionophore A23187A J Dessein, T H Lee, P Elsas, et al.Neurology|January 30, 2008
Neuropathy progression in Charcot-Marie-Tooth disease type 1AM E Shy, L Chen, E R Swan, et al.Advances in Biophysics|January 1, 1991
Two-dimensional time resolved X-ray diffraction of muscle: recent resultsJ Bordas, G P Diakun, J E Harries, et al.American Journal of Human Genetics|December 1, 1999
Delineation of the critical interval of Bardet-Biedl syndrome 1 (BBS1) to a small region of 11q13, through linkage and haplotype analysis of 91 pedigreesN Katsanis, R A Lewis, D W Stockton, et al.Pageof 41